Canonical Allele Identifier: CA10649168
Community Standard Title: NM_001004334.4(GPR179):c.2556C>T (p.Leu852=)
Gene: GPR179 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38331013G>A , CM000679.2:g.38331013G>A GRCh38
NC_000017.9:g.33740422G>A NCBI36
NG_032655.2:g.17798C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001004334.4:c.2556C>T MANE Select NP_001004334.3:p.Leu852=
ENST00000616987.5:c.2556C>T MANE Select ENSP00000483469.2:p.Leu852=
NM_001004334.3:c.2556C>T NP_001004334.3:p.Leu852=
ENST00000616987.4:c.2556C>T ENSP00000483469.1:p.Leu852=
ENST00000621958.1:c.2559C>T ENSP00000480024.1:p.Leu853=
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